Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Christoph Rüdinger"'
Publikováno v:
Macromolecules. 56:1033-1044
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::def5a64f252ab9b5680e2d1f4d9d3d07
https://doi.org/10.1021/acs.macromol.2c01653
https://doi.org/10.1021/acs.macromol.2c01653
Publikováno v:
Applied Energy. 239:1242-1249
Oxymethylene ether (OMEn) has recently drawn high attention due to its high pollutant emission reduction potential and the sustainable synthesis pathways involving carbon capture and renewable hydrogen. In this work, five blends of OMEn in diesel fue
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::edfb3dee97095530fc70f5e8f5b5e739
https://doi.org/10.1016/j.apenergy.2019.02.035
https://doi.org/10.1016/j.apenergy.2019.02.035
Autor:
Helmut Papp, Michal Lutecki, Ekaterina M. Sadovskaya, Wladimir Suprun, Christoph Rüdinger, Hans-Jürgen Eberle
Publikováno v:
Applied Catalysis A: General. 391:125-136
The role of water in the oxidation of 1-butene to AcOH over VOx-TiO 2 was investigated using spectroscopic and transient isotopic exchange methods. It was shown that the influence of water strongly depended on the temperature of reaction. In particul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::117935d734d68b23b16fdfd9229f82ba
https://doi.org/10.1016/j.apcata.2010.03.043
https://doi.org/10.1016/j.apcata.2010.03.043
Publikováno v:
Applied Catalysis A: General. 269:237-248
In situ-FTIR, in situ-UV–vis and operando-EPR spectroscopic methods were used to study the interaction of 1-butene/N2, 1-butene/O2/N2 and 1-butene/O2/N2/H2O mixtures with VOx/TiO2 (6.1 wt.% V) and VOx/SbOy/TiO2 (4.2 wt.% V, 9.5 wt.% Sb) catalysts u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6216b9baad113881c1368ee2cae80ce
https://doi.org/10.1016/j.apcata.2004.04.027
https://doi.org/10.1016/j.apcata.2004.04.027
Publikováno v:
Zeitschrift für Naturforschung B. 49:1348-1360
Disilylacetylene (1) has been obtained from LiAlH4 reduction of bis(trichlorosilyl)acetylene (2) and bis[(trifluoromethylsulfonyloxy)silyl]acetylene (4). The catalytic hydrosilylation of 2 with HSiCl3 affords tris(trichlorosilyl)ethene (5) and 1.1.2-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b30bf5d8f62cdc54f2592a80d81ee918
https://doi.org/10.1515/znb-1994-1008
https://doi.org/10.1515/znb-1994-1008
Autor:
Norbert W. Mitzel, David W. H. Rankin, Christoph Rüdinger, Heather E. Robertson, Blair F. Johnston, Hubert Schmidbaur
The structures of 1,3,5-trisilylbenzene and hexasilylbenzene in the gas phase have been determined by electron diffraction, and that of 1,3,5-trisilylbenzene by X-ray crystallography. The structures of three trisilylbenzene isomers, three tetrasilylb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b35d4a8347a79ee9d16ca8a0b264aa3b
https://strathprints.strath.ac.uk/10627/1/303741.pdf
https://strathprints.strath.ac.uk/10627/1/303741.pdf
Autor:
Sarah L. Hinchley, Lorna J. McLachlan, David W. H. Rankin, Hubert Schmidbaur, Norbert W. Mitzel, Heather E. Robertson, Carole A. Morrison, Christoph Rüdinger
The molecular structures of trans-1,2-dichloro-1,2-disilylethene and 1-bromo-1-silylethene have been determined by gas-phase electron diffraction (GED) and ab initio molecular orbital calculations (MP2/6-311G). Both compounds were found to have highl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::289a8793153749c1ca1023dc1e848ffc
https://pub.uni-bielefeld.de/record/1928700
https://pub.uni-bielefeld.de/record/1928700
Publikováno v:
Chemische Berichte. 125:1401-1403
The title compound was obtained in a four-step synthesis starting from (4-methoxyphenyl)silane. Owing to the presence of activating p-methoxy groups in the key intermediate hexakis[(4-methoxyphenyl)silyl]benzene (4), the peripheral aryl groups can be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd51d3469e3620b98ff97cfbc534daf9
https://doi.org/10.1002/cber.19921250616
https://doi.org/10.1002/cber.19921250616